A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv807252



Internal ID16101208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:31954821..31964231hg38UCSC Ensembl
Innerchr13:32528958..32538368hg19UCSC Ensembl
Innerchr13:31426958..31436368hg18UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg389411
hg199411
hg189411
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561403
Supporting Variants
Samples
Known GenesEEF1DP3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv807252
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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